OMOP Concept 4148748
Stromal cell hyperplasia in androgen insensitivity syndrome
StandardConditionSNOMED270369000Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Stromal cell hyperplasia in androgen insensitivity syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 270369000 | Stromal cell hyperplasia in androgen insensitivity syndrome | Non-standard |
Synonyms
Alternative names recorded for Stromal cell hyperplasia in androgen insensitivity syndrome across source vocabularies.
- hiperplasia de células del estroma en el síndrome de insensibilidad a andrógenos
- hiperplasia de células del estroma en el síndrome de insensibilidad a andrógenos (trastorno)
- Stromal cell hyperplasia in androgen insensitivity syndrome (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(41)Roll up to these when you need a wider cohort.
- 1Androgen resistance syndrome
- 246,XY disorder of sex development
- 2Congenital anomaly of endocrine gonad
- 2Developmental hereditary disorder
- 2Disorder of androgen receptor
- 2Hereditary disorder of endocrine system
- 2Reproductive system hereditary disorder
- 2X-linked recessive hereditary disease
- 3Congenital anomaly of endocrine gland
- 3Congenital malformation of genital organs
- 3Developmental disorder
- 3Disorder of endocrine gonad
- 3Disorder of endocrine receptor
- 3Disorder of endocrine system
- 3Disorder of reproductive system
- 3Disorder of steroid metabolism
- 3Endocrine andrology disorder
- 3Gonadal dysgenesis
- 3Hereditary disease
- 3Hereditary disorder by system
- 3X-linked hereditary disease
- 4Congenital malformation
- 4Disease
- 4Disorder of body system
- 4Disorder of the genitourinary system
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